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FDA 510(k)

WATER BATH

K-Number: K822564 · 1982-09-14

Decision Date1982-09-14
Product CodeJTQ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

WATER BATH is the device name listed in this FDA 510(k) record. The listed applicant is Boekel Industries, Inc.. It received FDA 510(k) clearance on 1982-09-14 under 510(k) number K822564. The device is classified under product code JTQ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WATER BATH?

WATER BATH is a medical device that received FDA 510(k) clearance on 1982-09-14. The listed applicant is Boekel Industries, Inc.. The 510(k) number is K822564.

When did WATER BATH receive FDA 510(k) clearance?

WATER BATH received FDA 510(k) clearance on 1982-09-14, under 510(k) number K822564.

Who is the listed applicant for WATER BATH?

The FDA 510(k) record lists Boekel Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WATER BATH?

The FDA product code for WATER BATH is JTQ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Boekel Industries, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: JTQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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